Deferasirox
- Product NDC
- 0480-7011
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Deferasirox
- Dosage form
- TABLET, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals, Inc.
- Application
- ANDA207124
- Marketing category
- ANDA
- Substance
- DEFERASIROX
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 0480-7011-56 | 30 TABLET, FOR SUSPENSION in 1 BOTTLE (0480-7011-56) | 2024-11-01 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Deferasirox | Teva Pharmaceuticals, Inc. | 2024-07-01 | HUMAN PRESCRIPTION DRUG LABEL | 7 |